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Prognostic significance of autoantibodies for idiopathic pulmonary fibrosis: protocol for a systematic review
INTRODUCTION: Idiopathic pulmonary fibrosis(IPF) is chronic fibrosing interstitial pneumonia of unknown aetiology. IPF is diagnosed based on the exclusion of known causes such as connective tissue diseases(CTDs). However, some patients fail to meet defined CTD criteria regardless of an implication o...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | BMJ Open |
|---|---|
| Prif Awduron: | , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BMJ Publishing Group
2018
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5855166/ https://ncbi.nlm.nih.gov/pubmed/29523572 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2017-020862 |
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